Treponema pallidum pallidum

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Treponema pallidum pallidum /
Revision as of 19:58, 7 May 2020 by Aidan (talk | contribs) (: added latent section for relapses)
  • Causes syphilis

Background

Microbiology

  • Small, slow-growing spirochete
  • Not seen on standard microscopy; requires darkfield microscopy

Clinical Presentation

Stages

  • Primary syphilis (incubation period 3 weeks [range 3 to 90 days])
  • Secondary syphilis (incubation period 2 weeks to 3 months [range 2 weeks to 6 months])
  • Latent
    • Early latent (<1 year)
    • Late latent (≥1 year)
  • Tertiary syphilis (incubation period years to decades)
    • Cardiovascular (incubation period 10 to 30 years)
    • Gummatous (incubation period 15 years [range 1 to 46 years])
    • Neurosyphilis (incubation period 2 to 20 years)
      • Meningovascular
      • Parenchymatous
      • Tabes dorsalis
  • Congenital
    • Early (< 2 years)
    • Late (≥ 2 years)

Primary syphilis

  • Incubation period is about 3 weeks
  • Chancre
  • Ulcerative lesion
    • Clean borders
    • Indurated
    • Not painful unless secondarily infected
    • Lasts 2 to 6 weeks
  • May present with regional lymphadenopathy
  • Diagnosis with darkfield microscopy, fluorescent antibody smear, or (most commonly) serology
  • Serology often negative in early syphilis

Secondary syphilis

  • Incubation period 3 weeks to 3 months
  • Often no history of chancre
  • Diffuse maculopapular rash that involves palms and soles
    • Typically begins on trunk
    • Start as pinkish-reddish macular lesions that evolve into brownish-reddish papules that may have scaling
    • May progress to pustular lesions (pustular syphilids)
    • May be itchy
    • Can be isolated to palms and soles
  • Generalized lymphadenopathy
  • Fever, chills, arthralgias
  • Less common: condyloma lata, aseptic meningitis, iritis, mucosal white patches, glomerulonephritis, paroxysmal nocturnal hemoglobinuria, hepatitis

Latent syphilis

  • High rate of relapse of secondary syphilis within the first 1-2 years following infection (but especially within the first year)

Tertiary syphilis

  • Eventually occurs in about 30% of untreated cases

Neurosyphilis

  • Of the 25-60% of people who have CNS invasion, 95% are asymptomatic during the early stage and 80% of those spontaneously clear it
  • Incubation period is 7-15 years
  • Three major presentations: meningovascular syphilis, parenchymous syphilis, and tabse dorsalis
Meningovascular
  • Possibly the most common neurosyphilis
  • Subdivided into cerebromeningeal (diffuse or focal) and cerebrovascular
  • Stroke-like symptoms, especially MCA or basilar territory
  • Can present as a sudden change, as syphilitic apoplexy
  • Can present following a prodrome of weeks to months of non-specific headaches, vertigo, irritability, insomnia, and personality changes
Parenchymatous
  • Previously known as "generalized paresis of the insane"
  • Occurs in 2-5% of cases of untreated syphilis
  • Commonly found on psychiatric wards
  • Causes psychosis and dementia
  • Later, coarse tremors, Argyll-Robinson pupil, paresis
Tabes dorsalis
  • Occurs in 2-9% of cases of untreated syphilis
  • Isolated posterior cord degeneration leading to a loss of proprioception in the lower extremities
  • Stomp the ground when walking to use intact pain/pressure sensation
  • Loss of sensation in the Hitzig zones (tip of nose, band including nipple area, medial forearms, and lateral leg)
  • Can present with Charcot foot and, rarely, recurrent abdominal pain
  • Diagnosed by serum CMIA, but RPR may be negative
Others
  • Isolated ocular neurosyphilis
  • Meningitis: can present at any time during the course of disease
  • Others

Cardiovascular syphilis

  • Occurs in 10% of people with untreated syphilis
  • Incubation period is 20-25 years
  • Aortic root involvement leading to aortitis and dilatation
  • May result in aneurysm, aortic insufficiency, or angina secondary to stenosis at the aortic root
  • Diagnosed by RPR +/- CMIA

Gummatous syphilis

  • Occurs in 15% of people with untreated syphilis
  • Incubation period 6-8 years
  • Gummas may appear anywhere, in any organ
  • CNS lesions look like toxo, so beware in HIV patients

Other presentations

  • Isolated auditory syphilis
  • Isolated optic syphilis

Latent syphilis

  • Most common form of syphilis is latent, at any stage

Diagnosis

  • Often done as non-treponemal test to screen, followed by treponemal test to confirm
  • In Ontario, we do a treponemal test to screen (CMIA), then repeat it with a more specific treponemal test (TPPA) alongside RPR

Direct visualization

  • Darkfield microscopy
    • Chancre cleaned and smear obtained
    • Smear must be visualized immediately
    • Sensitivity decreases with duration
  • Smear for fluorescent monoclonal antibody
    • Best to use in primary syphilis

Non-treponemal tests (VDRL/RPR)

  • Veneral Diseases Research Laboratory (VDRL) has been replaced by the rapid plasma reagin (RPR) test
    • Quantitative tests for a non-specific anti-cardiolipin antibody that is produced in syphilitic (and other) infections
  • False positives in pregnancy, autoimmune disorders (lupus, APLA), and chronic infections (leishmaniasis, leprosy, ...)
  • 50% sensitive in primary, 100% sensitive in secondary
  • Tests will eventually become nonreactive

Treponemal tests

  • More specific and sensitive, but more expensive
  • False positive in lupus and Lyme disease
  • Remain positive for life
  • Four main tests:
    • Fluorescent treponemal antibody absorption (FTA-Abs): Essentially the gold standard
    • Chemoluminescnence microparticle immunoassay (CMIA or CLIA): the screening test used in Ontario. Often used as a screening test as it is an easily-automated immunoassay and is more sensitive and specific than RPR.
    • Treponema pallidum Particulate Agglutination assay (TPPA): a modification of the TPHA. Used as the confirmatory test (alongside RPR) used in Ontario.
    • T. pallidum hemagglutination assay (TPHA): very old test.
    • T. pallidum enzyme immunassay (TP-EIA)

Interpretation of serology

CMIA screen RPR TPPA Interpretation
Non-reactive Negative result; or early syphilis (consider repeat in 4 weeks)
Reactive Reactive Reactive Recent or prior syphilis infection
Reactive Non-reactive Reactive Recent or prior syphilis infection
Reactive Non-reactive Non-reactive False positive; or early syphilis, previously treated, or late latent (repeat in 4 weeks)
Reactive Non-reactive Indeterminate Inconclusive result; false positive, early syphilis, old treated syphilis, or old untreated syphilis (repeat in 4 weeks)
Reactive Reactive Non-reactive Inconclusive result; false positive, early syphilis, old treated syphilis, or untreated syphilis (repeat in 4 weeks)
Reactive Reactive Indeterminate Recent or prior syphilis infection

Treatment

Primary, secondary, and early latent

  • Benzathine penicillin G 2.4 million units IM once, divided between two buttocks
  • Alternative (penicillin allergy): doxycycline 100mg BID for 2 weeks
  • Alternative (penicillin allergy and pregnancy): penicillin desensitization or azithromycin

Late latent and tertiary (excluding neurosyphilis)

  • Benzathine penicillin G 2.4 million units IM q1week for 3 weeks
  • Alternative (penicillin allergy): doxycycline for 30 days
  • Monitor response with RPR titres, which should drop 4-fold within 6 months

Tertiary neurosyphilis

  • Penicillin G 4 million units IV q4h for 10 to 14 days
  • Often followed by at least one dose of IM benzathine penicillin, sometimes weekly for 2-3 weeks

Congenital syphilis

  • If <1 month of age: crystalline penicillin G 50 kU/kg IV q12h for the first week of life and q8h thereafter, for a total of 10 days
  • If ≥1 month of age: crystalline penicillin G 50,000 units/kg IV every 6 hours for 10-14 days
    • If there is no neurological involvement, then you can consider benzathine penicillin G 50 kU/kg (max 2.4 MU) IM weekly for 3 weeks